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Details

Stereochemistry ABSOLUTE
Molecular Formula C7H13NO3S
Molecular Weight 191.248
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-ACETYLMETHIONINE

SMILES

CSCC[C@H](NC(C)=O)C(O)=O

InChI

InChIKey=XUYPXLNMDZIRQH-LURJTMIESA-N
InChI=1S/C7H13NO3S/c1-5(9)8-6(7(10)11)3-4-12-2/h6H,3-4H2,1-2H3,(H,8,9)(H,10,11)/t6-/m0/s1

HIDE SMILES / InChI

Molecular Formula C7H13NO3S
Molecular Weight 191.248
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Specific reaction of Met 35 in amyloid beta peptide with hypochlorous acid.
2010-07
Formation and hydrolysis of amide bonds by lipase A from Candida antarctica; exceptional features.
2010-02-21
A bulky platinum triamine complex that reacts faster with guanosine 5'-monophosphate than with N-acetylmethionine.
2010-02
X-ray spectroscopic approaches to the investigation and characterization of photochemical processes.
2009-07
Synthesis, cellular uptake and structure-activity relationships for potent cytotoxic trichloridoiridium(III) polypyridyl complexes.
2008-08
Characterization of a bifunctional aminoacylase/carboxypeptidase from radioresistant bacterium Deinococcus radiodurans R1.
2007-02-01
The role of N-acetyl-methioninate as a new stabilizer for albumin products.
2007-02-01
Density functional theory methods as powerful tools to elucidate amino acid oxidation mechanisms. A case study on methionine model peptide.
2007-01-18
In vivo metabolism of L-methionine in mice: evidence for stereoselective formation of methionine-d-sulfoxide and quantitation of other major metabolites.
2006-12
Probing the catalytic center of porcine aminoacylase 1 by site-directed mutagenesis, homology modeling and substrate docking.
2006-03
Interaction of N-acetylmethionine with a non-C2-symmetrical platinum diamine complex.
2005-11
Purification and characterization of a novel aminoacylase from Streptomyces mobaraensis.
2005-10
Effects of geometric isomerism in dinuclear antitumor platinum complexes on their interactions with N-acetyl-L-methionine.
2005-08
Pyridine-carboxylate complexes of platinum. Effect of N,O-chelate formation on model bifunctional DNA-DNA and DNA-protein interactions.
2005-07-25
Methionine radical cation: structural studies as a function of pH using X- and Q-band time-resolved electron paramagnetic resonance spectroscopy.
2005-07-07
Potential roles of flavin-containing monooxygenases in sulfoxidation reactions of l-methionine, N-acetyl-l-methionine and peptides containing l-methionine.
2005-01-17
Molecular cloning and biochemical characterization of L-N-carbamoylase from Sinorhizobium meliloti CECT4114.
2005
Structural basis for catalytic racemization and substrate specificity of an N-acylamino acid racemase homologue from Deinococcus radiodurans.
2004-09-03
Evolution of enzymatic activity in the enolase superfamily: structural studies of the promiscuous o-succinylbenzoate synthase from Amycolatopsis.
2004-05-18
Kinetic analysis of the reactions of hypobromous acid with protein components: implications for cellular damage and use of 3-bromotyrosine as a marker of oxidative stress.
2004-04-27
Effect of amine ligand bulk on the interaction of methionine with platinum(II) diamine complexes.
2004-02-09
Evolution of enzymatic activity in the enolase superfamily: functional studies of the promiscuous o-succinylbenzoate synthase from Amycolatopsis.
2004-01-13
Free radical reactions of methionine in peptides: mechanisms relevant to beta-amyloid oxidation and Alzheimer's disease.
2003-11-12
Temperature dependence of the kinetics of the acylase hydrolysis reaction by differential stopped flow microcalorimetry.
2003-10-01
Identification and characterization of a new gene from Variovorax paradoxus Iso1 encoding N-acyl-D-amino acid amidohydrolase responsible for D-amino acid production.
2002-10
Importance of product inhibition in the kinetics of the acylase hydrolysis reaction by differential stopped flow microcalorimetry.
2002-09-15
L-methionine inhibits reaction of DNA with anticancer cis-diamminedichloroplatinum(II).
2002-09-10
Control of cytochrome C redox potential: axial ligation and protein environment effects.
2002-05-15
Cystathionine pathway-dependent cytotoxicities of diethyl maleate and diamide in rat and human hepatoma-derived cell cultures.
2002-02-06
Specific enhancement of acylase I and acylpeptide hydrolase activities by the corresponding N-acetylated substrates in primary rat hepatocyte cultures.
2002-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:47:34 GMT 2025
Edited
by admin
on Mon Mar 31 17:47:34 GMT 2025
Record UNII
9J12WX5B6A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-ACETYLMETHIONINE
MI  
Systematic Name English
ACETYL METHIONINE
INCI  
INCI  
Preferred Name English
METHIONIN
Systematic Name English
Acetylmethionine [WHO-DD]
Common Name English
THIOMEDON
Common Name English
ACETYL-L-METHIONINE
Systematic Name English
NSC-118514
Code English
N-ACETYLMETHIONINE [MI]
Common Name English
ACETYLMETHIONINE
WHO-DD  
Systematic Name English
N-ACETYL-L-METHIONINE [FCC]
Common Name English
METHIONINE, N-ACETYL-, L-
Systematic Name English
FOLLICUSAN
Brand Name English
L-(N-ACETYL)METHIONINE
Common Name English
L-METHIONINE, N-ACETYL-
Systematic Name English
N-ACETYL-L-2-AMINO-4-(METHYLTHIO)BUTYRIC ACID
Common Name English
METHIONINE, N-ACETYL-, L
Common Name English
N-ACETYL-L-METHIONINE
FCC  
Systematic Name English
METHIONAMINE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 172.372
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
Code System Code Type Description
NSC
118514
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
PUBCHEM
448580
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
SMS_ID
100000077932
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
ECHA (EC/EINECS)
200-617-7
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
CAS
65-82-7
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
DRUG BANK
DB01646
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
MERCK INDEX
m1362
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY Merck Index
EVMPD
SUB12722MIG
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
RXCUI
1426463
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY RxNorm
MESH
C006379
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
CHEBI
16811
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID00883214
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
DAILYMED
9J12WX5B6A
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
CHEBI
21557
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
FDA UNII
9J12WX5B6A
Created by admin on Mon Mar 31 17:47:34 GMT 2025 , Edited by admin on Mon Mar 31 17:47:34 GMT 2025
PRIMARY
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